FDA PMA FDA Class 3 Approved 🇺🇸 United States

System, Hemodynamic, Implantable

PMA: P100045 · Supplement: S049 · Decision Sep 21, 2021
Classifications
1
FEI Numbers
9
Registration Numbers
9

Basic Information

Device Name
System, Hemodynamic, Implantable
Trade Name
CardioMEMS HF System
PMA Number
P100045
Supplement Number
S049
Device Class
FDA Class 3
Product Code
MOM
Generic Name
System, hemodynamic, implantable
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
September 21, 2021
Date Received
March 2, 2021
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the next generation CardioMEMS Hospital System (CM3100).

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MOM System, Hemodynamic, Implantable